savastanoi pathovar examined. The specificity of these primer pairs, named PsvRT-F/PsvRT-R, PsnRT-F/PsnRT-R, PsfRT-F/PsfRT-R (Table 2), was preliminarily assessed by BLAST analysis. Then these primer sets were tested in Real-Time PCR runs with SYBR® Green as fluorescent marker and 1 μl of DNA template extracted from 1 ml of titrated suspensions (corresponding to about 103 to 107 CFU/reaction) of strains Psv ITM317, Psn ITM519 and Psf NCPPB1464. Since SYBR® Green binds to the minor grooves of a DNA double-chain as it is forming, this fluorescent dye can bind to all amplicons

produced in a PCR reaction. Therefore, the specificity of detection can be provided by a pair of primers only when the increase in fluorescence is generated by a single amplicon with a distinct melting temperature (Tm). For this reason TPCA-1 dissociation analysis is crucial in SYBR® Green PCR BAY 1895344 experiments. The melting curves obtained with the primer pairs developed in this study are shown in Figure 3. Figure 3 Melting temperature analysis and quantitative standard curves of SYBR ® Green Real-Time PCR assays.(A) primer set PsvRT-F/PsvRT-R on

strain Psv ITM317; (B) primer set PsnRT-F/PsnRT-R on strain Psn ITM519; (C) primer set PsfRT-F/PsfRT-R on strain Psf NCPPB1464. Quantitative thermal dissociation curves were represented plotting fluorescence derivative values [-d (fluorescence units)/d (time)] versus temperature, obtained with DNA from the target P. savastanoi Erastin datasheet pathovar, extracted by thermal lysis from 103 to 107 CFU per reaction (red, orange, yellow, green and blue lines, respectively) and with no target DNAs (blue diamond), extracted from the two other P. savastanoi pathovars,

from olive (A), oleander (B) and ash (C) and from a pool of bacterial unidentified epiphytes isolated from the same plants (from olive, oleander and ash in A, B and C, respectively). Standard curves were generated by plotting the Ct values versus the log of genomic DNA concentration of each tenfold dilution series in the range of linearity (from 50 ng to 5 pg per reaction). The Ct data obtained with target DNA from 103 to 107 CFU per reaction were reported (+). (See online for a colour version of this figure). For all the five different cell concentrations a single melting Olopatadine peak at 85.5°C (± 0.1) was observed with the primer pair PsvRT-F/PsvRT-R and DNA extracted from isolate Psv ITM317, to indicate that the total fluorescent signal was contributed by specific amplicons. No signals were recorded in melting point analysis with the set PsvRT-F/PsvRT-R in DNA-free control and when no target DNAs were used as template (Figure 3). The pair PsnRT-F/PsnRT-R obtained a similar specificity, giving a unique melting peak at 85.0°C (± 0.1) only with DNA from strain Psn ITM519, as well as the primer set PsfRT-F/PsfRT-R that originated a single peak at 86.5°C (± 0.1) only with DNA from strain Psf NCPPB1464.